Canonical Allele Identifier: CA1770294904

Gene: BMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22201457C= , CM000670.2:g.22201457C=	GRCh38
NC_000008.10:g.22058970C= , CM000670.1:g.22058970C=	GRCh37
NC_000008.9:g.22114915C=	NCBI36
NG_029659.1:g.41318C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306349.13:c.*254C= MANE Plus Clinical	ENSP00000306121.8:n.*254C=
ENST00000306385.10:c.2108-346C= MANE Select	ENSP00000305714.5:n.2108-346C=
ENST00000520626.6:c.*2294C=	ENSP00000430015.2:n.*2294C=
ENST00000306349.12:c.*254C=	ENSP00000306121.8:n.*254C=
ENST00000306385.9:c.2108-346C=	ENSP00000305714.5:n.2108-346C=
ENST00000354870.5:c.*1365-346C=	ENSP00000346941.5:n.*1365-346C=
ENST00000518913.5:c.*1914C=	ENSP00000427950.1:n.*1914C=
ENST00000520626.5:c.*2294C=	ENSP00000430015.1:n.*2294C=
ENST00000520970.5:c.*254C=	ENSP00000428332.1:n.*254C=
ENST00000520982.5:c.*1575-346C=	ENSP00000428798.1:n.*1575-346C=
ENST00000522332.1:n.1312C=
NM_001199.3:c.*254C=	NP_001190.1:n.*254C=
NM_006129.4:c.2108-346C=	NP_006120.1:n.2108-346C=
NR_033403.1:n.2411-346C=
NR_033404.1:n.2750C=
XR_949458.1:n.2481-346C=
XR_001745579.2:n.2655C=
XR_949458.2:n.2423-346C=
NM_006129.5:c.2108-346C= MANE Select	NP_006120.1:n.2108-346C=
NM_001199.4:c.*254C= MANE Plus Clinical	NP_001190.1:n.*254C=
NR_033403.2:n.2179-346C=
NR_033404.2:n.2518C=